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Deuruxolitinib

Phase 3

Alopecia Areata | Small molecule | Dermatology |Pulmonx Corporation|Last Updated: Aug 18, 2026

Success Probability

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Market & Valuation

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Trial Design

RandomizedDouble-BlindPLACEBO_CONTROLLED
Total Trials1
Total Enrollment78

FDA Designations

No designations recorded

Clinical trial landscape

Deuruxolitinib · 1 trial · 1 indication

Phase 3 1
NCT07617597Study to Evaluate the Efficacy and Safety of Deuruxolitinib in Japanese Adults With Severe Alopecia AreataAlopecia Areata
RECRUITING78 Analytics
PHASE3RECRUITING
Study to Evaluate the Efficacy and Safety of Deuruxolitinib in Japanese Adults With Severe Alopecia Areata
Alopecia AreataUnlock trial analytics

Study Endpoints

Primary Endpoints

Percentage of subjects achieving an absolute SALT score of 20 or less
Week 24

SALT is a quantitative assessment of scalp hair loss with scores ranging in severity from 0 (no scalp hair loss) to a maximum of 100 (complete scalp hair loss).

Secondary Endpoints

Percentage of responders (defined as "satisfied" or "very satisfied") on the Satisfaction of Hair Patient Reported Outcome (SPRO) scale
Week 24
Percentage of subjects achieving an absolute SALT score of 20 or less
Weeks 12, 16, and 20
Relative change in SALT scores from baseline
Weeks 4, 8, 12, 16, 20, and 24
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Study Design & Arms

AllocationRANDOMIZED
MaskingQUADRUPLE
ModelPARALLEL
PurposeTREATMENT

Treatment Arms

ArmTypeDescription
Deuruxolitinib 8 mgEXPERIMENTALParticipants in this arm will receive deuruxolitinib 8 mg administered orally twice daily (BID) during the 24-week double-blind treatment period and continue to receive deuruxolitinib 8 mg administered orally BID up to 52 weeks
PlaceboPLACEBO_COMPARATORParticipants in this arm will receive matching placebo administered orally BID during the 24-week double-blind treatment period and then receive deuruxolitinib 8 mg administered orally BID up to 52 weeks.

Interventions

NameTypeDescription
DeuruxolitinibDRUGDeuruxolitinib will be dosed orally as tablets at a dose of 8 mg
PlaceboDRUGDeuruxolitinib matching placebo will be dosed orally as tablets for up to 24 weeks and then deuruxolitinib will be dosed for up to 52 weeks
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Eligibility Criteria

Age Range18 Years to 65 Years
SexALL
Healthy VolunteersNo
Study Sites18

Inclusion Criteria: * Written informed consent has been obtained. * Japanese subjects with severe alopecia areata who are between 18 and 65 years of age, inclusive, at the time of informed consent. * Definitive diagnosis of alopecia areata with a current episode of scalp hair loss lasting at least ...

Countries:Japan
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